Document Detail


Intravenous implanted neural stem cells migrate to injury site, reduce infarct volume, and improve behavior after cerebral ischemia.
MedLine Citation:
PMID:  20560882     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Stroke represents one of the leading causes of death and disability in humans, but despite intense research, only a few options exist for the treatment of stroke-related infarction of brain tissue. Thus far, in experimental strokes, cell therapy appears to partly reverse some behavioral deficits. However, the mechanisms of action remain uncertain as most studies reveal only little, if any, evidence for neuronal replacement and observed behavioral improvements. This present study was performed to test rodent fetus forebrain derived neural stem cells (NSCs) implantation into rats subjected to suture-induced middle cerebral artery occlusion (MCAO). Efficacy of cell therapy was studied regarding behavior recovery, infarct volume, and protection possibility of related molecular mechanisms. Here, we show that grafted cells can home in on damaged regions by MCAO and significantly improve behavior of ischemic rats. Infarct volumes and brain atrophy were diminished after grafted NSCs treatment. Furthermore, we detected inflammation related molecules such as COX-2 and IL-1beta and found that grafted NSCs treatment after ischemic stroke could repress expression of inflammation molecular protein levels. We also detected protein levels of heat shock protein 27 (HSP27) as a protective protein against apoptosis. The results showed that grafted NSCs treatment induced the protein level of HSP27 and down-regulated activity of caspase-3 compared with the vehicle control. Our results demonstrate that transplanted NSCs provide benefits in behavioral function recovery after MCAO and increase neuroprotection whilst repressing inflammatory destruction. These data reveal another essential explanation of cellular transplantation therapy in damage recovery from ischemic stroke and offer new therapeutic possibilities.
Authors:
Chiung-Chyi Shen; Chen-Huan Lin; Yi-Chin Yang; Ming-Tsang Chiao; Wen-Yu Cheng; Jiunn-Liang Ko
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Current neurovascular research     Volume:  7     ISSN:  1875-5739     ISO Abbreviation:  Curr Neurovasc Res     Publication Date:  2010 Aug 
Date Detail:
Created Date:  2010-08-04     Completed Date:  2010-11-12     Revised Date:  2011-06-07    
Medline Journal Info:
Nlm Unique ID:  101208439     Medline TA:  Curr Neurovasc Res     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  167-79     Citation Subset:  IM    
Affiliation:
Department of Neurosurgery, Taichung Veterans General Hospital, Taichung, Taiwan.
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MeSH Terms
Descriptor/Qualifier:
Analysis of Variance
Animals
Blotting, Western
Brain Ischemia / metabolism,  pathology,  physiopathology,  therapy*
Caspase 3 / metabolism
Cell Movement*
Cyclooxygenase 2 / metabolism
HSP27 Heat-Shock Proteins / metabolism
Hand Strength
Immunohistochemistry
Interleukin-1beta / metabolism
Neurons / cytology,  transplantation
Rats
Rats, Wistar
Recovery of Function
Stem Cell Transplantation*
Stem Cells / metabolism
Stroke / metabolism,  pathology,  physiopathology,  therapy*
Chemical
Reg. No./Substance:
0/HSP27 Heat-Shock Proteins; 0/Hspb1 protein, rat; 0/Interleukin-1beta; EC 1.14.99.1/Cyclooxygenase 2; EC 3.4.22.-/Caspase 3

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